EP1648471A2 - Methodes de traitement de dysfonctionnements sexuels masculins et feminins - Google Patents

Methodes de traitement de dysfonctionnements sexuels masculins et feminins

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Publication number
EP1648471A2
EP1648471A2 EP04780074A EP04780074A EP1648471A2 EP 1648471 A2 EP1648471 A2 EP 1648471A2 EP 04780074 A EP04780074 A EP 04780074A EP 04780074 A EP04780074 A EP 04780074A EP 1648471 A2 EP1648471 A2 EP 1648471A2
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EP
European Patent Office
Prior art keywords
cds
cyclodextrin
medicament
amount
levels
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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EP04780074A
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German (de)
English (en)
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EP1648471A4 (fr
Inventor
Nicholas S. Bodor
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Ivax LLC
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Ivax LLC
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Publication of EP1648471A4 publication Critical patent/EP1648471A4/fr
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/12—Drugs for genital or sexual disorders; Contraceptives for climacteric disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/30—Oestrogens
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery

Definitions

  • the invention relates to methods for the treatment of female and male sexual dysfunction using a brain-targeted delivery system for estradiol, namely 17 ⁇ -[(l- methyl- 1 ,4-dihydro-3 -pyridinyl)carbonyloxy] estra- 1,3,5(10)-trien-3 -ol, also known as E 2 -CDS, and use of E 2 -CDS in the preparation of a medicament for treating male and female sexual dysfunction.
  • Sexual dysfunction in men includes, in the main, erectile dysfunction, male orgasmic disorder, inhibited or hypoactive sexual desire and priapism.
  • Inhibited or hypoactive sexual desire refers to a decrease in desire for, or interest in, sexual activity and can result from a variety of causes, including physical illness, depression, hormonal abnormality or medications that affect libido.
  • Male sexual behavior is composed of proceptive and consummately behaviors. The proceptive behaviors include the awareness of the presence of a receptive female, the pursuit of that female and the positioning of the body (mounting) to allow insertion of the penis into the vagina.
  • testosterone replacement can restore the full expression of the behavior [Davidson et al., in S. Levine (Ed.) Hormones and Behavior, Academic Press, New York, 1972, pp. 63-103].
  • Several lines of evidence indicate that the proceptive components of masculine sexual behavior are dependent upon the aromatization in the brain of testosterone to estradiol.
  • estradiol appears as the major androgen metabolite in regions of the brain known to mediate masculine sexual behavior.
  • [ 3 H] -testosterone was administered systemically and sections of the brain were extracted to determine the steroid metabolites present.
  • hypothalamus preoptic area and amygdala, 50% or more of the radioactivity was reported to be estradiol, while in other brain structures, the radioactivity remained as testosterone.
  • estradiol stimulates the proceptive components of masculine sexual behavior. Pfaff (J. Comp. Physiol. Psych.
  • estradiol benzoate administered estradiol benzoate systemically (10 ⁇ g/day) for 9 to 11 days to castrated male rats and observed that estradiol increased mounting, intromissions and ano-genital sniffing and reduced mounting latency to levels comparable to that observed following the administration of testosterone propionate (200 ⁇ g/day).
  • Sodersten Hormones and Behavior 4: 247-256, 1973
  • estradiol benzoate 100 ⁇ g/day
  • the normal female sexual response cycle is now divided into four stages: desire, excitement, orgasm, and resolution.
  • Female sexual dysfunction may occur at any one, or more than one, stage of the female sexual response cycle.
  • Consensus classifications and definitions, based on the stages of normal female sexual response are divided into four broad categories: sexual desire disorders, sexual arousal disorders, orgasmic disorders, and sexual pain disorders; of these four, the most common is hypoactive (inhibited) sexual desire disorder (HSDD).
  • HSDD is defined as persistent or recurrent deficiency (or absence) of sexual fantasies, thoughts, and/or desire for, or receptivity to, sexual activity, which causes personal distress.
  • Estradiol E 2
  • Ruggiero and Likis J. Midiwifery and Women's Health, 47(3), 103-138 (2002).
  • Many of estradiol's pharmacological effects are mediated through the CNS.
  • Brain-specific steroid deprivation causes syndromes such as male or female sexual dysfunction and menopausal vasomotor symptoms ("hot flushes"); see Greendale et al, Lancet, 353, 571-580 (1999); Yen, J. Reprod. Med. 18(6), 287-296 (1977).
  • sexual dysfunction may be closely linked to and include symptoms associated with the estrogen deprivation of menopause, such as vaginal dryness/lack of lubrication and consequent pain associated with intercourse, which can be closely associated in turn with diminished sexual desire.
  • CDS brain-targeted chemical delivery system
  • a centrally acting drug [D] is coupled to a quaternary carrier [QC] + through a reactive functional group (such as a hydroxyl function) in the drug; the [D-QC] + which results is then reduced chemically to the lipoidal dihydro form [D-DHC].
  • a reactive functional group such as a hydroxyl function
  • the [D-QC] + which results is then reduced chemically to the lipoidal dihydro form [D-DHC].
  • the dihydro form [D-DHC] is then in situ oxidized (by the NAD ⁇ NADH system) to the ideally inactive original [D-QC] + quaternary salt which, because of its ionic, hydrophilic character, is rapidly eliminated from the general circulation of the body, while the blood-brain barrier prevents its elimination from the brain.
  • E 2 -CDS is a specific CDS devised for estradiol which is described in these patents.
  • the lipophilic 17-dihydrotrigonelline ester of estradiol i.e., E 2 -CDS
  • E 2 -Q + hydrophilic trigonellinate ester
  • the hydrophilic E 2 -Q + form is thus "locked-in” the brain and is slowly and sustainedly hydrolyzed by esterases to estradiol (E 2 ).
  • Similar E 2 -CDS ⁇ E 2 -Q + conversion in the rest of the body accelerates peripheral elimination and improves targeting.
  • E 2 -CDS has been previously suggested for a number of uses, including treatment of male sexual dysfunction (Anderson et al U.S. Patent No. 4,863,911) and weight control (Bodor et al. U.S. Patent No. 4,617,298), as well as brain-specific, steroid deprivation syndromes (such as hot flushes) and for chronic reduction of gonadotropin secretion for fertility regulation (contraception) or treatment of gonadal steroid-dependent diseases, such as endometriosis and prostatic hypertrophy (noted in column 46 of Bodor et al. U.S. Patent No. 4,617,298).
  • Experiment 3 examined the dose-response of LH inhibition in ovariectomized rats on day 12 post-drug treatment following a single i.v. dose of 0J, 0.5, 2.0 or 5.0 mg/kg of E 2 -CDS; of 0.07, 035, 1.38, 3.46 or 10.38 mg/kg estradiol; or of DMSO vehicle (0.5 mg/kg). Blood samples were collected on day 12 post-treatment.
  • Experiment 4 compared a single i.v. dose of 0.5 mg/kg E 2 -CDS with equimolar estradiol 17-valerate for LH inhibition, and blood samples were collected on day 12 or 18 post-treatment.
  • Serum LH was decreased by 75% and 91% compared to vehicle at the 2 or 5 mg/kg dosage, respectively, of E 2 -CDS, in Experiment 3.
  • the dose of 0.5 mg/kg gave heterogeneous results and therefore was reexamined in Experiment 4.
  • LH was significantly decreased by E -CDS compared to estradiol valerate. No serum estradiol analyses were done in the female tests. In the castrated male rat, a single i.v.
  • E 2 -CDS showed very high serum estradiol at early time points of 4 and 8 hours (>1000 pg/ml), and elevated levels for several days post-treatment, but not at 12, 18 and 24 days post- treatment, while LH levels remained very significantly reduced at 12, 18 and 24 days post-treatment.
  • Anderson et al, Life Sciences 42, 1493-1502 (1988) reported tests in ovariectomized female rats in which the rats received an intravenous injection of E 2 - CDS at 10, 33, 100 or 333 ⁇ g/kg or the vehicle DMSO, 0.5 ml/kg, every two days for seven injections (2 weeks) or a single injection only 2 days before sacrifice.
  • the single dose of E 2 -CDS caused dose-dependent reduction in serum LH (39-52%) at
  • Ovariectomized rats received single or multiple i.v. doses of E 2 -CDS at 1.0 mg/kg or E 2 (0.5 mg pellet) weekly for 1 to 3 weeks before temperature recording.
  • a single 1 mg/kg i.v. injection of E 2 -CDS attenuated the naloxone-induced rise in TST by 25% when tested one week after injection but that amount was not statistically significant.
  • Plasma E 2 concentrations were increased to 1.9 ⁇ 0.08 ng/ml (1900 ⁇ 80 pg/ml) 30 minutes after E 2 -CDS administration, then decreased by 50% at 3 hours and more than 91% at 24 hours post-treatment.
  • the authors noted that the morphine-dependent naloxone-withdrawal rat model was to their knowledge the only animal model available to evaluate the effectiveness of E 2 -CDS for treatment of hot flushes, but also questioned whether this model is actually analogous to menopausal hot flushes since in some animals (50% or less) the E 2 -treatment did not completely stabilize. If the model were truly consistent with the estrogen deprivation which results in hot flushes, the performance of estrogens in the test would have been more consistent.
  • FSH and 17 ⁇ -estradiol (E 2 ).
  • Minimal effects on plasma LH were found in the 10-40 ⁇ g dose group, threshold effects in the 80-640 ⁇ g dose group and substantial and sustained decreases in plasma LH in the 1280 ⁇ g dose group.
  • one post-menopausal human volunteer receiving a single 1280 ⁇ g i.v. dose of E 2 -CDS was found to have LH lowered in a "clinically meaningful" way through 96 hours after E 2 -CDS administration.
  • E 2 -CDS was a potent, long- acting stimulant of the proceptive components of masculine sexual behavior.
  • the Anderson et al. patent suggested use of E 2 -CDS alone if deficits in peripheral androgen-responsive tissues were not an issue; in other cases, administration together with an androgen such as testosterone was suggested.
  • Such an amount of 3 mg/kg is generally 10 times the mg/kg amount expected to be comparable in humans.
  • a 0.3 mg/kg amount was expected to provide comparable results in men.
  • a first aspect of the present invention there is provided use of the compound 17 ⁇ -[(l-methyl-l,4-dihydro-3-pyridinyl)carbonyloxy]estra-l,3,5(10)- trien-3-ol in the preparation of a medicament for treating female sexual dysfunction in a female mammal, said compound being present in said medicament in an amount effective to diminish symptoms of said dysfunction which does not elevate average steady-state peripheral estradiol levels to above about 50-60 pg/ml.
  • a second aspect of the present invention there is provided use of the compound 17 ⁇ -[(l -methyl- 1 ,4-dihydro-3-pyridinyl)carbonyloxy]estra-l ,3,5(10)- trien-3-ol in the preparation of a medicament for treating female sexual dysfunction in a woman, said compound being present in said medicament in an amount effective to diminish or alleviate symptoms of said dysfunction which does not elevate average steady-state peripheral estradiol levels to above about 50-60 pg/ml.
  • the invention provides use of the compound 17 ⁇ -[(l- methyl- 1 ,4-dihydro-3-pyridinyl)carbonyloxy]estra- 1 ,3,5(10)-trien-3-ol in the preparation of a medicament for treating postmenopausal symptoms in a postmenopausal woman, said compound being present in said medicament in an amount effective to diminish or alleviate said symptoms which does not elevate average steady-state peripheral estradiol levels to above about 50-60 pg/ml.
  • the foregoing aspects of the invention further comprise use of repeated daily or every other day dosing of amounts as small as about 0.01 mg/kg or lower (about 0.5 to about 2.0 mg per day in postmenopausal women) via buccal administration, i.e.
  • a buccal dosage unit containing the indicated amount of E 2 -CDS via a buccal dosage unit containing the indicated amount of E 2 -CDS, and/or without elevation of average steady-state estradiol peripheral levels in such women to above about 40 pg/ml, even about 20 pg/ml or lower, and/or with average peak estradiol peripheral levels (which are reached shortly after administration) in such women not above about 70-90 pg/ml or even lower, and/or using the active compound in cyclodextrin, particularly as a substantially saturated complex with hydroxypropyl- ⁇ -cyclodextrin (to achieve the highest degree of thermodynamic activity).
  • the compound 17 ⁇ -[(l-methyl-l,4-dihydro-3-pyridinyl)carbonyloxy]estra-l,3,5(10)- trien-3-ol in the preparation of a medicament for treating male sexual dysfunction in a man, said compound being present in said medicament in an amount effective to diminish or alleviate symptoms of said dysfunction which does not substantially elevate average peripheral estradiol levels to above average normal levels in men.
  • the foregoing aspects of treating male sexual dysfunction further comprise repeated daily or every other day dosing of amounts comparable to 0.01 mg/kg i.v.
  • in the castrated male rat for example, amounts of about 0.01 to about 0.5 mg per day buccally to men, i.e. via a buccal dosage unit containing the indicated amount of E 2 -CDS, for such period of time as required until symptoms diminish (for example, approximately 2 to 7 days in men), with resumption of daily or every other day dosing when symptoms recur, and/or administering the active compound in cyclodextrin, particularly as a substantially saturated complex with hydroxypropyl- ⁇ -cyclodextrin (to achieve the highest degree of thermodynamic activity).
  • FIG. 1 is a plot of lordosis quotient (percent responders) versus time in days for varying doses of estradiol-CDS, i.e., 17 ⁇ -[(l -methyl- l,4-dihydro-3- pyridinyl)carbonyloxy]estra-l,3,5(10)-trien-3-ol (E 2 -CDS), at 0.003 mg/kg (A),
  • ⁇ 0.01 mg/kg ( ⁇ ), 0.03 mg/kg (•), and of the control vehicle, hydroxypropyl- ⁇ - cyclodextrin (HP ⁇ CD) solution ( ⁇ ), in ovariectomized female rats after daily intravenous (i.v.) injections for five days, with observations beginning on day 3 following the first injection.
  • HP ⁇ CD hydroxypropyl- ⁇ - cyclodextrin
  • FIG. 2 is a plot of lordosis quotient (percent responders) versus time in days for varying doses of estradiol benzoate, at 0.003 mg/kg ( ⁇ ), 0.01 mg/kg (0) and 0.03 mg/kg (O), and of the control vehicle, hydroxypropyl- ⁇ -cyclodextrin (HP ⁇ CD) solution (D), in ovariectomized female rats after daily intravenous (i.v.) injections for five days, with observations beginning on day 3 following the first injection.
  • FIG. 3 is a group of three (3) plots of lordosis quotient (percent responders) versus time in days for the same doses as in FIGs.
  • FIG. 4 is a plot of LH levels in ng/ml plasma versus time in days for varying doses of E 2 -CDS at 0.003 mg/kg (•), 0.01 mg/kg (A), 0.03 mg/kg ( ⁇ ), and of the control ( ⁇ ) in ovariectomized female rats after daily single i.v. tail injections for five days, with observations beginning on day 3 following the first injection.
  • FIG. 4 is a plot of LH levels in ng/ml plasma versus time in days for varying doses of E 2 -CDS at 0.003 mg/kg (•), 0.01 mg/kg (A), 0.03 mg/kg ( ⁇ ), and of the control ( ⁇ ) in ovariectomized female rats after daily single i.v. tail injections for five days, with observations beginning on day 3 following the first injection.
  • FIG. 4 is a plot of LH levels in ng/ml plasma versus time in days for varying doses of E 2 -CDS at 0.003 mg/kg
  • FIG. 5 is a plot of LH levels in ng/ml plasma versus time in days for varying doses of estradiol benzoate at 0.003 mg/kg (•), 0.01 mg/kg (A), 0.03 mg/kg ( ⁇ ), and of the control ( ⁇ ) in ovariectomized female rats after daily single i.v. tail injections for five days, with observations beginning on day 3 following the first injection.
  • FIG. 6 is a bar graph illustrating the effect of varying doses of estradiol-CDS
  • E 2 -CDS at 0.03 mg/kg (0), 0.3 mg/kg (S), 3.0 mg/kg ( ⁇ ), and of the control vehicle, hydroxypropyl- ⁇ -cyclodextrin (HP ⁇ CD) solution (D), on the mounting performance (% responders) in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35, after a single intravenous (i.v.) injection.
  • HP ⁇ CD hydroxypropyl- ⁇ -cyclodextrin
  • FIG. 7 is a bar graph illustrating the effect of varying doses E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S) and 3.0 mg/kg ( ⁇ ) and of the control vehicle, HP ⁇ CD ( ⁇ ), on the intromission percentage (% responders) in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • E 2 -CDS 0.03 mg/kg (0), 0.3 mg/kg (S) and 3.0 mg/kg ( ⁇ ) and of the control vehicle, HP ⁇ CD ( ⁇ ), on the intromission percentage (% responders) in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 8 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S), and 3.0 mg/kg ( ⁇ ) and of the control vehicle HP ⁇ CD (D), on the mounting frequency in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 8 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S), and 3.0 mg/kg ( ⁇ ) and of the control vehicle HP ⁇ CD (D), on the mounting frequency in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 9 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S) and 3 mg/kg ( ⁇ ), and of the control vehicle HP ⁇ CD (D), on the mounting latency, in minutes, in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 10 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S) and 3 mg/kg ( ⁇ ), and of the control vehicle HP ⁇ CD (D), on the intromission frequency in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 10 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg (S) and 3 mg/kg ( ⁇ ), and of the control vehicle HP ⁇ CD (D), on the intromission frequency in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 11 is a bar graph and accompanying chart illustrating the effect of varying doses of E 2 -CDS, at 0.03 mg/kg (0), 0.3 mg/kg ( ⁇ ) and 3 mg/kg ( ⁇ ) and of the control vehicle HP ⁇ CD (D), on the intromission latency, in minutes, in intact male rats, and in castrated male rats at days 0, 3, 7, 14, 21, 28 and 35 after a single intravenous (i.v.) injection.
  • FIG. 12 is a plot of LH levels in ng/ml plasma versus time in days for varying doses of E 2 -CDS at 0.03 mg/kg (x), 0.3 mg/kg ( ⁇ ) and 3 mg/kg (A) and of the control vehicle HP ⁇ CD (•) in orchidectomized (castrated) male rats for a period of 35 days after a single intravenous (i.v.) injection).
  • FIG. 13 is a bar graph illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v. once daily for 10 days, and the control vehicle, HP ⁇ CD (D), on the mounting performance (% responders) in intact male rats, and in castrated male rats at days 0, 1, 3, 7, 14 and
  • FIG. 14 is a bar graph illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v. once daily for 10 days, and the control vehicle, HP ⁇ CD (D), on the intromission performance (% responders) in intact male rats, and in castrated male rats at days 0, 1, 3, 7, 14 and 21.
  • FIG. 15 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v.
  • FIG. 16 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v. once daily for 10 days, and the control vehicle, HP ⁇ CD(D), on the mounting latency, in minutes, in intact male rats, and in castrated male rats at days 0, 1, 3, 7, 14 and 21.
  • FIG. 17 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v.
  • FIG. 18 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v. once daily for 10 days, and the control vehicle, HP ⁇ CD (D), on the intromission frequency (number of intromissions) in intact male rats, and in castrated male rats at days 0, 1, 3, 7, 14 and 21.
  • FIG. 18 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS administered i.v. once, and 0.01 mg/kg (B) E 2 -CDS administered i.v. once daily for 10 days, and the control vehicle, HP ⁇ CD (D), on the intromission frequency (number of intromissions) in intact male rats, and in castrated male rats at days 0, 1, 3, 7, 14 and 21.
  • FIG. 18 is a bar graph and accompanying chart illustrating the effect of 0.03 mg/kg (0) E 2 -CDS
  • complex means an inclusion complex, in which a hydrophobic portion of the E 2 -CDS molecule (typically a portion of the steroidal ring system) is inserted into the hydrophobic cavity of the cyclodextrin molecule.
  • a hydrophobic portion of the E 2 -CDS molecule typically a portion of the steroidal ring system
  • HP ⁇ CD it is believed that in the 1 :1 complex, the aromatic A ring of the steroid is included.
  • a 1 :2 complex of E 2 -CDS:HP ⁇ CD forms and the second HP ⁇ CD molecule may interact with the dihydronicotinate group in the E 2 -CDS molecule.
  • the terms “comprise(s)” and “comprising” are to be inte ⁇ reted as having an open-ended meaning. That is, the terms are to be interpreted synonymously with the phrases “having at least” or “including at least”.
  • the term “comprising” means that the process includes at least the recited steps, but may include additional steps.
  • the term “comprising” means that the composition includes at least the recited features or components, but may also include additional features or components.
  • the basic and novel features herein are the provision of methods for treating male and female sexual dysfunction in which the amount of E 2 -CDS administered is carefully controlled so that it diminishes symptoms in an amount which does not elevate average steady-state peripheral estradiol levels to above average normal peripheral levels in the male, or which does not elevate average steady-state peripheral estradiol levels to above about 50-60 pg/ml in the female.
  • the methods comprise buccal administration of an anhydrous formulation of a substantially saturated complex of the compound 17 ⁇ -[(l-methyl-l,4-dihydro-3-pyridinyl)carbonyloxy]estra-l, 3,5(10)- trien-3-ol with a hydroxyalkyl, carboxyalkyl or carboxymethylethyl derivative of ⁇ - or ⁇ -cyclodextrin comprising from about 0.01 to about 0.5 mg of said compound per day in men and from about 0.5 to about 2.0 mg of said compound per day in women.
  • the terms "consists of and "consists” are closed terminology and allow only for the inclusion of the recited steps or features or components.
  • saturated when used in conjunction with a complex of E 2 -CDS in cyclodextrin means that the complex is saturated with the E 2 -CDS, that is, the complex contains the maximum amount of the E 2 -CDS which can be complexed with a given amount of cyclodextrin under the conditions of complexation used.
  • a phase solubility study can be used to provide this information.
  • a saturated complex may be arrived at empirically by simply adding the E 2 -CDS to an aqueous solution of the selected cyclodextrin until a precipitate (of uncomplexed E 2 -CDS) forms; ultimately, the precipitate is removed and the solution lyophilized to provide the dry saturated complex.
  • substantially means that from 80% to 100%, preferably from 90% to 100%, of the complex is in saturated form. In any other context, “substantially” similarly means within 20% of the exact calculated amount, preferably within 10% of that amount. Whatever the context, within 5% of the calculated amount is most desirable.
  • the recitation of a numerical range for a variable is intended to convey that the invention may be practiced with the variable equal to any of the values within that range. Thus, for a variable which is inherently discrete, the variable can be equal to any integer value of the numerical range, including the end- points of the range.
  • variable can be equal to any real value of the numerical range, including the end- points of the range.
  • a variable which is described as having values between 0 and 2 can be 0, 1 or 2 for variables which are inherently discrete, and can be 0.0, 0J, 0.01, 0.001, or any other real value for variables which are inherently continuous.
  • the singular forms include plural referents unless the context clearly dictates otherwise.
  • peripheral estradiol levels refers to serum estradiol levels obtained throughout the treatment period, using repeated dosing on a once per day or every other day schedule.
  • steady-state peripheral estradiol levels refers to serum estradiol levels obtained throughout the treatment period, using repeated dosing on a once per day or every other day schedule, excluding initial peak levels obtained within 1-2 hours after the initial dose.
  • lordosis refers to vertebral dorsiflexion performed by female quadrupeds in response to adequate stimuli from a reproductively competent male.
  • the lordosis quotient is calculated as 100 x number of lordoses/10 mounts.
  • mounting and "intromission” are explained in the foregoing Background of the Invention.
  • male mammal is intended to include any male mammal but especially human beings, domestic and farm animals, zoo animals and rare or endangered or expensive mammalian species.
  • female mammal is intended to include any female mammal but especially human beings, domestic and farm animals, zoo animals and rare or endangered or expensive mammalian species.
  • Cavasol W8 HP in deionized 135 mL water (DIUF) to form an approximately 25% w/v solution. Adjust the pH to 8.4-9.6 with sodium carbonate 1% solution. Degas the solution by passing argon through it. Add slowly, drop-wise, under stirring and bubbling argon, at 20-25°C, a solution of E 2 -CDS (1.5 g) in ethanol (3 mL). Allow time after each addition for the solution to become clear. The addition takes about 4 hours and it is slower at the end. A clear solution will result. Evaporate the solution to dryness in a rotary evaporator (bath temperature 35°C). Reconstitute the residue in water, calculated to obtain the initial concentration of the cyclodextrin solution.
  • METHOD A Dissolve 100 mg of E 2 -CDS and 500 mg of O-carboxymethyl-O-ethyl- ⁇ - cyclodextrin (CME ⁇ CD) in 10 mL of ethanol and sonicate the solution for 1 hour.
  • CME ⁇ CD O-carboxymethyl-O-ethyl- ⁇ - cyclodextrin
  • the complex should contain about 25 mg E 2 -CDS/g.
  • METHOD B Dissolve 2 g of CME ⁇ CD in 20 mL of 0.10M pH 9.0 borate buffer. Adjust the pH with IN sodium hydroxide solution. Then dissolve 150 mg of E 2 -CDS in 2 mL of ethanol and add the resultant solution to the cyclodextrin solution. Stir for 3 hours at 0°C under argon, remove the solvent in vacuo, reconstitute the residue with pH 9 borate buffer and lyophilize.
  • a buccal tablet was designed for use in clinical trials to deliver E 2 -CDS transmucosally and thus avoid the instability of E 2 -CDS in gastrointestinal fluid, which leads to multiple decomposition productions starting with water addition and/or oxidation, as well as hepatic first pass metabolism.
  • Transmucosal abso ⁇ tion is highly effective from the invention's saturated complex of E 2 -CDS in HP ⁇ CD (as prepared, for example, in EXAMPLE 2 above) with minimal additives.
  • a placebo was also prepared for the clinical trials.
  • Similar buccal tablets can be prepared containing complexes of E 2 -CDS with other cyclodextrins such as HP ⁇ CD, CME ⁇ CD or other cyclodextrin identified in this specification.
  • estradiol acts in the hypothalamus and preoptic area to regulate the expression of lordosis, an important component of female reproductive behavior and a characteristic posture of the female for a sexually active male to allow copulation.
  • Estradiol acts on multiple molecular targets that may converge on common biochemical pathways to ensure integration of sensory and neurochemical cues that regulate lordosis expression.
  • lordosis was selected as an indicator of restoration of female sexual function in ovariectomized female rats and an appropriate indicator for alleviating symptoms of female sexual dysfunction.
  • Circulating luteinizing hormone is a biomarker reflecting the CNS effects of estradiol.
  • Estrogen diminishes the secretion of luteinizing hormone- releasing hormone (LHRH) and hence reduces the secretion of LH. Therefore, LH and estradiol levels were investigated to measure the central and peripheral effects of E 2 -CDS, respectively.
  • HP ⁇ CD solution (0.29 mg/kg is equimolar to that of 0.3 mg/kg E 2 -CDS).
  • E 2 -CDS as a 3% complex with HP ⁇ CD (E 2 -CDS-CD) was dissolved in distilled water and diluted with 27% HP ⁇ CD solution.
  • E 2 -CDS-CD was synthesized by Alchem Laboratories Co ⁇ oration, Alachua, FL, US. BEHAVIORAL TESTING After recovery from surgery, ovariectomized female rats were divided into four groups and treated once a day for five days intravenously, via a bolus injection through the tail vein, as follows: (1) control, 27% HP ⁇ CD solution; (2) 0.003 mg/kg
  • E 2 -CDS dissolved in 27% HP ⁇ CD solution (3) 0.01 mg/kg E 2 -CDS dissolved in 27% HP ⁇ CD solution; and (4) 0.03 mg/kg E 2 -CDS dissolved in 27% HP ⁇ CD solution.
  • a minimal number of ovariectomized (8 to 12) females were used per group.
  • Intravenous treatments either with E 2 -CDS or HP ⁇ CD (controls) were carried out daily for 5 days beginning 2 days prior to the first day of behavior observations, in a volume of 0.05 ml/100 g body weight.
  • the investigation of estradiol benzoate (EB) was performed in newly randomized previously ovariectomized females after a resting period of 3 weeks.
  • estradiol benzoate was dissolved in 40% HP ⁇ CD and diluted with 27% HP ⁇ CD solution (0J9 mg/kg stock solution equimolar to that of E 2 -CDS).
  • the behavior test was conducted in a plexiglass observation cage during the dark cycle. During behavioral observations, only a dim red light was on. An experienced and active male rat was placed in the arena 5 minutes prior to the female. Each female was observed for the time often successful mounts per test session or for a maximum of 10 minutes, and the number of lordosis responses was recorded.
  • Plasma estradiol levels were determined by double antibody I 125 isotope-RIA kits obtained from BioChem Immuno System. The limit of detection was 15 pg/ml. Behavioral changes were analyzed using the Mann- Whitney U test (Siegel, Nonparametric Statistics for the Behavioral Sciences, New York; McGraw-Hill
  • Serum LH data were analyzed for each time and treatment group by analysis of variance (ANON A) followed by Bonferroni posthoc test. Plasma LH and estradiol concentrations were evaluated by the computerized standard curve program of Prism software (Version 3.0, Graph Pad, San Diego, CA, US).
  • FIGs. 1-5 show the results obtained.
  • data are mean ⁇ SE for 8-12 animals per group; *p ⁇ 0.05, **p ⁇ 0.01, ***p ⁇ 0.001 using the Mann- Whitney U test.
  • data are mean ⁇ SE for 7-11 animals per group, with *, ** and *** as defined for FIG. 1.
  • the data presented in FIG. 1 and FIG. 2 are reorganized in FIG. 3 so as to more readily compare the effect of the same dose of E 2 -CDS and estradiol benzoate (E 2 -Benz).
  • data are mean ⁇ SE for 7-12 animals per group, *p ⁇ 0.05, **p ⁇ 0.01, ***p ⁇ 0.001 using A ⁇ OVA followed by the Bonferroni posthoc test.
  • the lordosis quotient LQ was significantly enhanced by both E 2 -CDS and estradiol benzoate.
  • E 2 -CDS this effect lasted from day 3 to day 18, as shown in FIG. 1.
  • the effect from estradiol benzoate was less pronounced and lasted only from day 3 to day 8; see FIG. 2.
  • the LQ value for estradiol benzoate was about three times lower than that obtained for E 2 -CDS: the maximal values of LQ after E 2 -CDS and estradiol benzoate treatments were 73 and 27.3 respectively.
  • E 2 -CDS significantly enhanced the LQ from day 5 to day 11.
  • This dose of estradiol benzoate slightly increased the LQ from day 3 to day 10 (about 3 times less compared to E 2 -CDS), but this effect was not statistically significant.
  • doses of the test compounds slightly enhanced the lordosis quotient, but these effects were not statistically significant (estradiol benzoate, days 3-7; E 2 -CDS, days 3-18). See FIGs. 1, 2 and the third portion of FIG. 3.
  • FIG. 4 shows that plasma LH levels were suppressed at all dosage levels of
  • E 2 -CDS tested i.e. at 0.003, 0.01 and 0.03 mg/kg. Even at the low i.v. dose of 0.03 mg/kg, the plasma LH level was suppressed in a statistically significant manner for up to 18 days; plasma LH suppression lasted for up to 15 days even for the very low dose of 0.003 mg/kg. In contrast, as shown in FIG. 5, none of the tested dosages of estradiol benzoate gave statistically significant LH suppression.
  • the foregoing studies show that E 2 -CDS can restore female sexual function in rats and indicate that symptoms of female sexual dysfunction can be alleviated through its administration to females, including women, at doses far lower than previously thought possible, while maintaining appropriate peripheral levels of estrogen.
  • E 2 -CDS has been studied in clinical trials of postmenopausal women given a single 2.5 mg or 5 mg dose of E 2 -CDS administered buccally. Even more recently, in a Phase I clinical study of postmenopausal women, two different administration regimens of a 2.86 mg E 2 -CDS buccal delivery tablet were evaluated for safety and effects on hormone levels. The subjects were 12 healthy postmenopausal volunteers, divided into two groups of six. In Group A, women were dosed once daily for 10 days (10 doses); in Group B, women were dosed once every other day for 13 days (7 doses).
  • Dissolution E 2 -CDS was administered in a buccal delivery form (a buccal tablet) as a saturated complex with hydroxypropyl- ⁇ -cyclodextrin.
  • the median buccal dissolution time was 11 minutes and 13 seconds
  • E 2 CTR max serum estradiol levels
  • E 2 concentration was 11.5 ⁇ 2.7 pg/mL in the every other day group, and 36.8 ⁇ 54.6 pg/mL in the once daily group, respectively. In the once daily group, this post-study value would be 12.5 ⁇ 6.5 pg/mL if the values for subject 12 are omitted. 3.
  • Estrone (Ej) Ei was measured during the first 24 hours along with E 2 and at post-study (i.e. 72 hours after the last dose).
  • the post-study values were 47.5 ⁇ 49.7 pg/mL (without subject 12: 27.8 ⁇ 12.8 pg/mL) and 31.4 ⁇ 9.4 pg/mL in the once daily, and in the every other day dosing regimen group, respectively.
  • a similar trough level pattern to E 2 without accumulation can be anticipated for Ei as well in both dosing regimen groups, i.e. a steady state at somewhat higher level for the once daily administration group, than for the once every other day group. 4.
  • LH suppression During the first 24 hours the maximum decrease in LH was 13.8 ⁇ 4.9 and 12.7 ⁇ 6.8 mlU/mL from baseline in Group A and B, respectively (Group A showed slightly higher baseline values).
  • Serum testosterone concentrations on day 1 decreased to 1.3 ⁇ 1.9 and 4.0 ⁇ 3.9 ng/dL from 22.5 ⁇ 21.0 and 24.0 ⁇ 14.0 ng/dL, in Group A and B, respectively.
  • the time to reach these minimum testosterone levels on day 1 were 6.5 ⁇ 11.7 and 7.3 ⁇ 11.3 hours in Group A and B, respectively.
  • 72 hours after the last administered dose testosterone levels returned and slightly exceeded those of baseline values by 14 and 28% in Group A and B, respectively. However, the differences between the two groups did not reach statistical significance in any parameter. 9.
  • I6OHE 1 The mean amounts of Ej and the ratios Ej/creatinine in the 24-hour urine on day 1 in both groups were very similar. Mean amounts and ratios of 2OHE ⁇ to I6OHE 1 in 8-hour urine on day 10 in Group A appeared slightly higher than in Group B on day 13. Consequently, the differences of mean amounts (adjusted to an 8-hour urine collection period) and differences of mean ratios of day 10 - 1 in Group
  • a four week pack of tablets analogous to those typically used for dispensing estrogen progestin combinations, e.g. Prempro ® , or oral contraceptives, could be used in either case, with the alternate day regimen simplified for patients by alternating E 2 -CDS buccal tablets with placebo tablets.
  • the occurrence of few adverse events among which only one was judged as reasonably attributable to the trial drug proves the excellent safety and tolerance of E 2 -CDS when buccally administered at a low dose.
  • the finding of an increase in the urinary 2OHE t to I6OHE 1 ratio indicates a good safety profile in terms of breast cancer risk as well. Data from literature has consistently proven that a lower urinary 2OHE ⁇ /16OHE ⁇ ratio represents an important biomarker for increased breast cancer risk.
  • E 2 -CDS Treatment with E 2 -CDS does not change the metabolism of E 2 and Ej in a way that would confer an increased risk for breast cancer, but on the contrary changes the ratio in a beneficial direction.
  • the metabolite profile is protective rather than harmful. Because these metabolites compete for the same estrogenic receptor, the increased amount of the "good metabolite” (2OHE ⁇ ) decreases the possibility that the "bad metabolite” (I6OHE 1 ) will occupy the estrogen receptor and initiate cellular events that can lead to mutations within breast epithelial cells.
  • a Phase II clinical trial (first efficacy study or proof-of-concept study) is under preparation.
  • This new clinical study is designed to evaluate primarily the effects of E 2 -CDS complexed with HP ⁇ CD and delivered by the buccal route (EstredoxTM), administered once daily (QD) at three dose levels (0.5 mg/day, 1.0 mg/day, and 2.0 mg/day), compared to placebo, during a 12-week treatment phase, on the number and severity of hot flashes as measured by the "hot flash daily weighted severity score" (DWSS) in patients suffering from moderate to severe postmenopausal vasomotor symptoms.
  • Secondary parameters to be evaluated are the placebo-controlled treatment effects on scores calculated from a Menopause Rating Scale (MRS) questionnaire in this patient population. Treatment compliance, and acceptability of the buccal formulation tablet will also be evaluated among the secondary parameters of the study.
  • MRS Menopause Rating Scale
  • Disintegration time of the buccal tablets will be recorded on Day 1, 28, and 26.
  • Safety indices before and after treatment will be evaluated too, and include physical examination with vital signs, routine safety laboratory tests, including hemostasis parameters, observed or reported adverse events, hormone levels as biomarkers of central estradiol effects, such as serum FSH, LH, prolactin, SHBG, E 2 , Ei, urinary E ⁇ and the ratio of urinary 2OHE[ and l ⁇ OHEj, endometrial thickness evaluated by TVS, Pap smear, vaginal cytology (maturation index) and pH, endometrial aspirate with Pipelle, and breast examination.
  • the primary objective of this study is the evaluation of the effect of QD EstredoxTM buccal tablet at doses of 0.5, 1.0, and 2.0 mg E 2 -CDS/day compared to placebo on the number and severity of hot flashes in ambulatory postmenopausal women suffering from moderate to severe vasomotor symptoms (hot flashes) during 12 weeks of treatment.
  • Secondary objectives include the evaluation of placebo-controlled effects of three doses of EstredoxTM (0.5, 1.0, and 2.0 mg E 2 -CDS/day) on the scores of the
  • EstredoxTM treatment is to be determined by measuring vital signs, routine laboratory, including hemostasis parameters, and biomarkers to confirm central estrogenic effects, such as serum FSH, LH, E 2 together with prolactin, SHBG, and Ei, urinary Ei and the ratio of urinary 2OHE ⁇ /16OHE ! before, during (except prolactin, SHBG, and urine - at weeks 4 and 8) and after the 12 weeks treatment period.
  • Patients are to also undergo detailed gynecological examinations including endometrial thickness by TVS, Pap smear, vaginal cytology (maturation index) and pH, endometrial aspirate with Pipelle, and breast examination (mammography and ultrasound) twice; i.e. before and after treatment (week 0 and 12).
  • This is to be a phase II multi-center, repeated administration, double-blind, placebo-controlled dose-range study involving 80 ambulatory postmenopausal female patients randomly assigned in equal numbers into one of four treatment groups.
  • Patients with an intact uterus who are not under current estrogen, or estrogen-progestogen (ET/EPT), phytoestrogen, or selective estrogen receptor modulator (SERM) therapy can be enrolled.
  • EPM estrogen-progestogen
  • SERM selective estrogen receptor modulator
  • E 2 -CDS in accord with the present invention can provide effective treatment of female sexual dysfunction, including effective treatment of postmenopausal symptoms, at doses far lower than previously expected to be effective for treating women with E 2 -CDS for postmenopausal symptoms.
  • No specific dosages were ever previously suggested for treating other aspects of female sexual dysfunction such as sexual desire disorders or sexual pain disorders; in fact, treatment of these aspects of female sexual dysfunction has not been previously proposed and no relevant animal testing has been described in the E 2 -CDS literature.
  • E 2 -CDS literature emphasizes the substantial and prolonged suppression of LH levels.
  • LH inhibition may be more important for certain uses of estrogens such as contraception, there does not appear to be a direct connection between LH suppression and treatment of sexual dysfunction.
  • the low levels of E 2 -CDS which can be effectively administered to women for the treatment of various aspects of sexual dysfunction in accord with this invention are particularly su ⁇ rising; the 0.5 to 2.0 mg daily buccal dose, assuming approximately 30% bioavailability, calculates to an actual useable dose of only 0J5 to 0.6 mg per day, which divided by an average 60-70 kg weight, gives an approximate 0.0025 to 0.01 or less mg/kg dose in women.
  • dosage amounts will vary with the route of administration and the bioavailability applicable to the selected route.
  • the particular conditions to be relieved by administration in accord with the present invention include female sexual dysfunction, especially of the hypoactive sexual desire disorder type or of the sexual pain disorder type, as well as the symptoms linked to those disorders in postmenopausal women, whether the symptoms are associated with age or with other causes of estrogen deprivation (such as surgery).
  • vaginal dryness/lack of lubrication and consequent pain associated with intercourse vasomotor symptoms such as night sweats and hot flushes, insomnia, depression, nervousness, urinary incontinence, irritability and anxiety, even fear of pain of intercourse, all of which may be associated with the hypoactive sexual desire disorder.
  • vasomotor symptoms such as night sweats and hot flushes
  • insomnia depression, nervousness, urinary incontinence
  • irritability and anxiety even fear of pain of intercourse, all of which may be associated with the hypoactive sexual desire disorder.
  • other conditions associated with the estrogen deprivation of menopause or postmenopause such as osteoporosis and Alzheimer's disease, are also expected to be diminished by administration of the low-dose E 2 - CDS formulations provided herein. And these dosages do not provide constant elevated peripheral estrogen levels comparable to pre-menopausal levels, such as produced by standard HRT therapy.
  • E 2 -CDS is believed to be effective in diminishing the symptoms indicated above in amounts which do not elevate average steady-state peripheral estradiol levels to above about 50-60 pg/ml.
  • an effective dosage level may be selected in which such average peripheral estradiol levels do not exceed 40 pg/ml, or even 20 pg/ml or lower, with average peak estradiol peripheral levels not above 70-90 pg/ml or even lower.
  • peripheral estradiol levels which are low enough (50-60 pg/ml, 40-50 pg/ml, 20 pg/ml or lower, steady-state) and not above an average of about 70-90 pg/ml peak to minimize estrogen exposure in women.
  • E 2 -CDS is a potent, long-acting stimulant of the proceptive components of masculine sexual behavior.
  • estradiol can interfere with ejaculation and the Anderson et al. patent and other publications relating to E 2 -CDS do not address the issue of estradiol levels resulting from E 2 -CDS administration as to the impact such levels may have on the treatment of all aspects of male sexual dysfunction, including erectile function.
  • the drug as used in males in the E 2 -CDS literature produces unacceptably high estradiol levels in the serum for extended periods of time.
  • Circulating luteinizing hormone (LH) is a biomarker reflecting the CNS effects of estradiol.
  • Estrogen diminishes the secretion of luteinizing hormone- releasing hormone (LHRH) and hence reduces the secretion of LH. Therefore, LH and estradiol levels were investigated to measure the central and peripheral effects of E 2 -CDS, respectively.
  • LHRH luteinizing hormone- releasing hormone
  • rats were divided into four groups and treated intravenously, via a single tail vein injection, with one of the following: group 1 : control (27% hydroxypropyl- ⁇ - cyclodextrin); group 2: 0.03 mg/kg E 2 -CDS; group 3: 0.3 mg/kg E 2 -CDS; and group 4: 3 mg/kg E 2 -CDS.
  • group 1 control (27% hydroxypropyl- ⁇ - cyclodextrin)
  • group 2 0.03 mg/kg E 2 -CDS
  • group 3 0.3 mg/kg E 2 -CDS
  • group 4 3 mg/kg E 2 -CDS.
  • Mating was observed during the dark cycle in a plexi observation cage in a room where only a dim red light was on. The male was placed in the observation cage 5 minutes prior to the female.
  • Mount latency (ML): the time from the introduction of the female to the initial mount or intromission; Intromission latency (IL): the time from introduction of the female to the first intromission; and Ejaculatory latency (EL): the time from the first intromission to ejaculation.
  • Sessions were considered negative if IL exceeded 15 minutes.
  • EL was only measured to check the result of castration, so as to select only those animals that showed an ejaculation latency greater than 15 minutes.
  • each male was tested every 5 days until four successive and consistent behavioral patterns were achieved. This pretesting lasted for about four weeks. Approximately half of the animals tested were deemed suitable for orchidectomy.
  • Estradiol benzoate and progesterone were obtained from Richter Pharmaceuticals, Ltd., Budapest, Hungary and from Sigma Chemical Co. Inc., Budapest, Hungary, respectively.
  • 2-Hydroxypropyl- ⁇ -cyclodextrin was purchased from Cerestar Inc., Hammond, Indiana, US.
  • E 2 -CDS as a 3% complex with HP ⁇ CD was dissolved in distilled water and diluted with 27% HP ⁇ CD solution.
  • E 2 -CDS-CD was synthesized by Alchem Laboratories Co ⁇ oration, Alachua, FL, US.
  • FIGs. 6-12 show the results obtained.
  • data are mean ⁇ SE for 8-12 animals per group; *p ⁇ 0.05, **p ⁇ 0.01, ***p ⁇ 0.001 using the Fisher exact test or the Mann- Whitney U test, as appropriate (Fisher exact test in FIGs. 6 and 7,
  • each point represents the mean ⁇ SEM of samples obtained from 8 to 13 rats.
  • Orchidectomy was found to be less effective in reducing mounting response (FIG. 6) than in reducing intromission response (FIG. 7).
  • E 2 -CDS restored mounting performance in 100% of the animals by day 7 at the dose of 0.3 mg/kg and by day 14 and day 21 at the dose of 3.0 mg/kg.
  • the intromission performance was improved in a statistically significant manner from day 14 through day 28 at the dose of 3.0 mg/kg.
  • Mount frequency was significantly increased on day 7 at doses of 0.3 and 3.0 mg/kg and on days 14, 21 and 28 at the dose of 3.0 mg/kg (FIG. 8).
  • E 2 -CDS tested At the lowest dose of E 2 -CDS tested (0.03 mg/kg i.v.), plasma LH levels were not reduced. At the dose of 0.3 mg/kg i.v., the title compound significantly reduced the LH levels on days 1, 3, and 7. By day 15, there was no significant difference in the LH levels between control and treated animals. At the highest dose of E 2 -CDS tested (3 mg/kg i.v.), LH levels were suppressed significantly throughout 28 days (FIG. 12). Estradiol levels were below the limit of detection in animals treated with E 2 - CDS at doses of 0.03 and 0.3 mg/kg i.v.
  • the estradiol level was 258 ⁇ 19 pg/ml on day 1 after treatment. At this dose, the hormone level decreased by 39% to 165 ⁇ 14 pg/ml on day 3 and to 61 ⁇ 7.7 pg/ml on day 7.
  • the estradiol level for the highest dose tested was below the limit of detection. See Table 1 below. This confirms that the dosage level of E 2 -CDS used in the Anderson et al. patent (3 mg/kg single i.v. dose in rats) would have produced unacceptably high peripheral estradiol levels for a prolonged period and agrees with data set forth in the Anderson et al. patent and in the E 2 -CDS literature. This level is expected to be high enough to interfere with ejaculation.
  • the plasma LH level was significantly reduced at the dose of 0.01 mg/kg (10 daily injections) from day 3 to day 14. At the dose of 0.03 mg/kg (single injection), the plasma LH level was significantly reduced on day 3 only.
  • the results of the repeated examination can be seen in FIG. 19.
  • animals were over-anesthetized, and the prostate and seminal vesicles were removed and their weights were measured.
  • the relative prostate and seminal vesicle weights are summarized in Table 2 below. Table 2.
  • Estradiol levels were below the limit of detection in all animals treated with E 2 -CDS at doses of 0.03 mg/kg (single dose) and 0.01 mg/kg (daily for 10 days) i.v. See Table 3 below.
  • E 2 -CDS can restore male sexual function in rats and indicate that symptoms of male sexual dysfunction in males, including men, can be alleviated through its administration at doses far lower than previously thought possible, while maintaining appropriate peripheral levels of estrogen.
  • Clinical studies in women substantiate that low dose buccal administration of E 2 -CDS can be correlated with animal test data and allow calculation of suitable buccal dosages for men based on the animal test data in male rats.
  • E 2 -CDS in accord with the present invention provides effective treatment of male sexual dysfunction, at doses far lower than previously expected to be effective for treating men with E 2 -CDS for male sexual dysfunction by using repeated small doses of the compound rather than the single dose once-a- month therapy suggested earlier, to minimize or obviate elevation of peripheral estradiol levels. It also is not necessary to use a dosage high enough to significantly reduce serum LH in order to effectively treat male sexual dysfunction.
  • the low levels of E 2 -CDS which can be effectively administered to men for these pu ⁇ oses are particularly su ⁇ rising; for example, a dose comparable to 0.01 to 0.001 mg/kg i.v.
  • this buccal dose calculates to an actual useable dose of only 0.003 to 0.015 mg per day, which divided by an average 70-80 kg weight, gives an approximate 0.0000375 to 0.00021 or less mg/kg dose in men.
  • Treatment is continued once-a-day or once every other day for such period of time as required until symptoms diminish, generally about 2 to 7 days in men, and treatment is resumed when symptoms recur.
  • dosage amounts will vary with the route of administration and the bioavailability applicable to the selected route.
  • E 2 -CDS in accord with the present invention will utilize dosage amounts and dosage frequencies which will not substantially elevate average peripheral estradiol levels to above average normal levels in the male, i.e., will not elevate average peripheral estradiol levels more than about 10-15% above normal levels. This in turn will prevent peripheral estradiol levels from inhibiting ejaculation, so that both proceptive and consummatory aspects of male sexual behavior will be improved.
  • E 2 -CDS can be administered by a variety of routes of administration and dosage forms which are already known from the various Bodor, Bodor et al and Anderson et al. patents referenced hereinabove, all of which are inco ⁇ orated by reference herein in their entireties and relied upon.
  • Pharmaceutical formulations for use in the methods of this invention comprise an amount of E 2 -CDS sufficient to diminish symptoms of female sexual dysfunction, including postmenopausal symptoms, which does not elevate average steady-state peripheral estradiol levels above about 50-60 pg/ml, or an amount of E 2 -CDS sufficient to diminish symptoms of male sexual dysfunction, which does not substantially elevate average peripheral levels above average normal peripheral levels in the male mammal.
  • the carrier and any other ingredients must of course be compatible with E 2 -CDS, and not detrimentally affect the effectiveness of the compound in treating female or male sexual dysfunction.
  • Suitable pharmaceutically acceptable carriers for use with E 2 -CDS are non- toxic and will be apparent to those skilled in the art of pharmaceutical formulation. See, e.g., Remington's Pharmaceutical Sciences, 17 th Ed., Gennaro, ed., Mack Publishing Company, Easton, Pa. (1985). The choice of suitable carriers will depend upon the exact nature of the particular dosage form selected, including of course the route of administration. The therapeutic dosage ranges for administration of E 2 -CDS for use in treating male and female sexual dysfunction has been detailed hereinabove. The dose selected will of course vary with the severity of the symptoms treated, the route of administration, the dosage form and the like.
  • Formulations according to the invention may be administered in any therapeutically effective manner, including, but not limited to, bucally, intranasally, sublingually, orally, topically (dermally), parenterally, by inhalation spray, vaginally or rectally in dosage unit formulations.
  • the pharmaceutical compositions according to the invention may be administered parenterally.
  • parenterally includes, but is not limited, to subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques.
  • the pharmaceutical composition may be in the form of a sterile injectable aqueous or oleagenous suspension. This suspension may be formulated according to known methods using those suitable dispersing or wetting agents and suspending agents which have been mentioned above.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example as a solution in 1 ,3-butanediol.
  • the acceptable vehicles and solvents include but are not limited to freshly prepared aqueous cyclodextrin solutions, particularly of hydroxyalkyl derivatives of ⁇ - or ⁇ -cyclodextrin or carboxyalkyl derivatives of ⁇ - or ⁇ -cyclodextrin or carboxymethylethyl ⁇ - or ⁇ -cyclodextrin or other suitable derivative, as discussed in more detail below.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • the pharmaceutical compositions according to the invention may be administered through buccal drug delivery.
  • buccal refers to delivery of a drug by passage of a drug through the buccal mucosa into the bloodstream.
  • Buccal drug delivery can be effected by placing the buccal dosage unit between the lower gum and the oral mucosa opposite thereto of the individual undergoing drug therapy.
  • Excipients or vehicles suitable for buccal drug administration can be used, and include any such materials known in the art, e.g., any liquid, gel, solvent, liquid diluent, solubilizer, or the like, which is nontoxic and does not interact with other components of the composition in a deleterious manner.
  • the dosage unit is fabricated so as to dissolve gradually over a predetermined time period, to produce a substantially saturated drug solution in the saliva of the buccal cavity, allowing abso ⁇ tion of E 2 -CDS through the mucosa, wherein drug delivery is provided essentially throughout the time period.
  • the buccal dosage unit may further comprise a lubricant to facilitate manufacture, e.g., magnesium stearate or the like.
  • the buccal dosage unit comprises the bioerodible polymeric carrier, and any excipients that may be desired, e.g., binders, disintegrants, lubricants, diluents, flavorings, colorings, and the like, and/or additional active agents.
  • the buccal carrier can comprise a polymer having sufficient tack to ensure that the dosage unit adheres to the buccal mucosa for the necessary time period, i.e., the time period during which the E 2 -CDS is to be delivered to the buccal mucosa.
  • the polymeric carrier is gradually “bioerodible", i.e., the polymer hydrolyzes at a predetermined rate upon contact with moisture.
  • Any polymeric carriers can be used that are pharmaceutically acceptable, provide both a suitable degree of adhesion and the desired drug release profile, and are compatible with the E 2 -CDS to be administered and any other components that may be present in the buccal dosage unit.
  • the polymeric carriers comprise hydrophilic (water- soluble and water-swellable) polymers that adhere to the wet surface of the buccal mucosa.
  • examples of polymeric carriers useful herein include acrylic acid polymers and copolymers, e.g., those known as "carbomers” for example, Carbopol®.
  • suitable polymers include, but are not limited to hydrolyzed polyvinyl alcohol, polyethylene oxides (e.g., Sentry Polyox®), polyacrylates (e.g., Gantrez®), vinyl polymers and copolymers, polyvinylpyrrolidone; dextran, guar gum, pectins, starches, and cellulosic polymers such as hydroxypropyl methylcellulose (e.g., Methocel®), hydroxypropyl cellulose (e.g., Klucel®), hydroxypropyl cellulose ethers, hydroxyethyl cellulose, sodium carboxymethyl cellulose, methyl cellulose, ethyl cellulose, cellulose acetate phthalate, cellulose acetate butyrate, and the like.
  • hydrolyzed polyvinyl alcohol polyethylene oxides (e.g., Sentry Polyox®), polyacrylates (e.g., Gantrez®), vinyl polymers and copolymers, polyvinylpyrrol
  • the dosage unit need contain only the E 2 -CDS and the carrier. However, it may be desirable in some cases to include one or more additional components.
  • a lubricant may be included to facilitate the process of manufacturing the dosage units; lubricants may also optimize erosion rate and drug flux. If a lubricant is present, it will represent on the order of 0.01 wt.% to about 2 wt.%, preferably about 0.01 wt.% to 0.5 wt.%, of the dosage unit.
  • Suitable lubricants include, but are not limited to, magnesium stearate, calcium stearate, stearic acid, sodium stearylfumarate, talc, hydrogenated vegetable oils and polyethylene glycol.
  • E 2 -CDS will most desirably be inco ⁇ orated into the buccal dosage form as a complex, preferably a substantially saturated complex, with a hydroxyalkyl or carboxyalkyl or carboxymethylethyl or other derivative of ⁇ - or ⁇ -cyclodextrin, as discussed in more detail hereinbelow.
  • E 2 -CDS may also be administered in accord with this invention in the form of a transdermal patch for transdermal administration of the drug.
  • the transdermal patches may include a variety of additional excipients which are conventionally employed to facilitate the transdermal administration of an active agent.
  • excipients include but are not limited to carriers, gelling agents, suspending agents, penetration-enhancing agents, dispersing agents, preservatives, stabilizers, wetting agents, emulsifying agents, and the like. Specific examples of each of these types of excipients are well-known in the art and any conventional excipients may be employed in the transdermal patches. Examples of suitable permeable surface layer materials are also well-known in the art of transdermal patch delivery, and any conventional material which is permeable to the E 2 -CDS to be administered.
  • suitable materials for the permeable surface layer include but are not limited to dense or microporous polymer films such as those comprised of polycarbonates, polyvinyl chlorides, polyamides, modacrylic copolymers, polysulfones, halogenated polymers, polychloroethers, acetal polymers, acrylic resins, and the like.
  • dense or microporous polymer films such as those comprised of polycarbonates, polyvinyl chlorides, polyamides, modacrylic copolymers, polysulfones, halogenated polymers, polychloroethers, acetal polymers, acrylic resins, and the like.
  • dense or microporous polymer films such as those comprised of polycarbonates, polyvinyl chlorides, polyamides, modacrylic copolymers, polysulfones, halogenated polymers, polychloroethers, acetal polymers, acrylic resins, and the like.
  • suitable penetration-enhancing agents are well known in the art as well.
  • Examples of conventional penetration-enhancing agents include alkanols such as ethanol, hexanol, cyclohexanol, and the like; hydrocarbons such as hexane, cyclohexane, isopropylbenzene, aldehydes and ketones such as cyclohexanone, acetamide, N,N- di(lower alkyl)acetamides such as N,N-diethylacetamide, N,N-dimethylacetamide, N-(2-hydroxyethyl)acetamide, esters such as N,N-di-(lower alkyl)sulfoxides, essential oils such as propylene glycol, glycerine, glycerol monolaurate, isopropyl myristate, and ethyl oleate, salicylates, and mixtures of any of the above.
  • alkanols such as ethanol, hexanol, cyclohexanol
  • E 2 -CDS is advantageously used in transdermal formulations as a complex, especially a substantially saturated complex, with a hydroxyalkyl or carboxyalkyl or carboxymethylethyl derivative of ⁇ - or ⁇ - cyclodextrin.
  • E 2 -CDS may also be administered in accord with this invention in the form of suppositories for vaginal or rectal administration.
  • compositions can be prepared by mixing E 2 -CDS (advantageously as a complex, especially a saturated complex, with hydroxypropyl- ⁇ -cyclodextrin, hydroxyethyl- ⁇ -cyclodextrin, the corresponding hydroxyethyl- ⁇ - or ⁇ -cyclodextrin derivative or the carboxymethyl or carboxyethyl or carboxymethylethyl derivative of ⁇ - or ⁇ -cyclodextrin) with a suitable non-irritating excipient or binder which is solid at ordinary temperatures but liquid at the vaginal or rectal temperature and will, therefore, melt in the vagina or rectum to release the drug.
  • suitable non-irritating excipient or binder which is solid at ordinary temperatures but liquid at the vaginal or rectal temperature and will, therefore, melt in the vagina or rectum to release the drug.
  • Such materials are cocoa butter and polyethylene glycols.
  • binders and carriers include, for example, polyalkylene glycols or triglycerides [e.g., PEG 1000 (96%) and PEG 4000 (4%)].
  • Such suppositories may be formed from mixtures containing active ingredients in the range of from about 0.5 wt/wt% to about 10 wt/wt%; preferably from about 1 wt/wt% to about 2 wt/wt%.
  • active ingredients in the range of from about 0.5 wt/wt% to about 10 wt/wt%; preferably from about 1 wt/wt% to about 2 wt/wt%.
  • creams, ointments, jellies, solutions or suspensions, etc. containing E 2 -CDS (desirably complexed with one of the cyclodextrin derivatives named in the preceding paragraph) can be employed.
  • a powder spray, suspension, gel or ointment may be utilized, preferably a powder form of E 2 -CDS, which may be complexed with one of the cyclodextrin derivatives discussed in the preceding two paragraphs. It will be apparent to those familiar with the patent and non-patent literature regarding E 2 -CDS, that complexation with cyclodextrin derivatives as well as formulation with such derivatives provides particularly useful dosage forms of E 2 - CDS for a variety of routes of administration. See, for example Bodor U.S. Patents
  • hydroxyethyl or hydroxypropyl derivatives of ⁇ - and ⁇ -cyclodextrin; carboxyalkyl, e.g. carboxymethyl or carboxyethyl, derivatives of ⁇ - or ⁇ -cyclodextrin; ⁇ -cyclodextrin sulfobutyl ether; carboxymethylethyl- ⁇ - or ⁇ -cyclodextrin; dimethyl- ⁇ -cyclodextrin; and randomly methylated ⁇ -cyclodextrin.
  • 2-Hydroxypropyl- ⁇ -cyclodextrin HP ⁇ CD
  • 2-hydroxypropyl- ⁇ -cyclodextrin HP ⁇ CD
  • randomly methylated ⁇ -cyclodextrin dimethyl- ⁇ -cyclodextrin, ⁇ -cyclodextrin sulfobutyl ether
  • carboxymethyl- ⁇ -cyclodextrin CM ⁇ CD
  • carboxymethyl- ⁇ -cyclodextrin CM ⁇ CD
  • carboxymethylethyl- ⁇ -cyclodextrin are of special interest, especially hydroxypropyl- ⁇ -cyclodextrin, hydroxypropyl- ⁇ - cyclodextrin, carboxymethyl- ⁇ -cyclodextrin and carboxymethyl- ⁇ -cyclodextrin.
  • a buccal dosage form for use in men or women, a buccal dosage form, especially a buccal tablet or wafer or disk, advantageously having a disintegration time of about 15-30 minutes, or a buccal patch (in which the drug is released only from the side which adheres to the buccal mucosa while the other side is nonpermeable), has particular advantages as it can be readily self-administered yet provides better bioavailability than oral dosage forms because the E 2 -CDS passes directly into the bloodstream from the buccal mucosa. (The cyclodextrin derivative is not absorbed, of course.)
  • the formulations for buccal administration are preferably anhydrous for reasons of storage stability.
  • HP ⁇ CD is also advantageously used in parenteral dosage forms for E 2 -CDS, both as a complexing agent and as a solvent as seen in the animal tests described hereinabove.
  • HP ⁇ CD, CM ⁇ CD or CM ⁇ CD, hydroxyethyl- ⁇ -cyclodextrin, hydroxyethyl- ⁇ -cyclodextrin, carboxyethyl- ⁇ - cyclodextrin or carboxyethyl- ⁇ -cyclodextrin may, for example, be used instead.
  • buccal administration may make use of the inventions of Nagai et al described in U.S.
  • a buccal mucosa-adhesive tablet may be formulated for use herein comprising: (a) a water-swellable and mucosa- adhesive polymeric matrix comprising about 50% to about 95% by weight of a cellulose ether and about 50% to about 95% by weight of a homo- or copolymer of acrylic acid or a pharmaceutically acceptable salt thereof, and (b) dispersed therein, an appropriate quantity of E 2 -CDS, typically from about 0.5 to 2.0 mg, as a substantially saturated complex with 2-hydroxypropyl- ⁇ -cyclodextrin.
  • the tablet is anhydrous.
  • one of the aforementioned other cyclodextrins e.g. hydroxyalkyl or carboxyalkyl or carboxymethylethyl ⁇ - or ⁇ - cyclodextrin derivatives, may be utilized in place of the 2-hydroxypropyl- ⁇ - cyclodextrin.
  • the buccal compositions according to the invention may optionally include one or more excipients or other pharmaceutically inert components, one of the advantages of these dosage forms when they comprise E 2 -CDS as a cyclodextrin complex is that they can be prepared with the minimal amount of excipients necessary for shaping and producing the particular form, such as a tablet or patch.
  • Excipients may be chosen from those that do not interfere with the E 2 -CDS, with cyclodextrin or with complex formation.
  • a simple solid buccal dosage form consists of the substantially saturated E 2 -CDS-cyclodextrin complex compressed with a small amount (e.g. about 1% by weight) of a suitable binder or lubricant such as magnesium stearate. Sorbitol may be added to the complex as well as magnesium stearate to aid in fast dissolution and to give good mouth feel.
  • the buccal dosage form may be a liquid.
  • a substantially saturated complex of E 2 -CDS in cyclodextrin in a minimum amount of water, for example 500 mg of the substantially saturated complex with HP ⁇ CD in 0.5 mL water (50% w/w solution), or 500 mg of the substantially saturated ⁇ CD complex in 1.0 mL of water.
  • a few drops of such a solution can be inserted into the buccal cavity and retained there for about 2 minutes to allow for abso ⁇ tion through the buccal mucosa.
  • solid buccal or other transmucosal dosage forms are generally preferred over liquid forms.

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Abstract

L'invention concerne l'utilisation de 17ß-[(1-méthyl-1,4-dihydro-3-pyridinyl)carbonyloxy]estra-1,3,5(10)-trién-3-ol, également appelé E2-CDS, pour préparer un médicament destiné à traiter un dysfonctionnement sexuel chez un mammifère femelle à l'aide de très faibles doses du composé n'entraînant pas d'augmentation des taux périphériques moyens d'estradiol stabilisé au-delà de 50-60 pg/ml environ. L'invention concerne aussi l'utilisation de E2-CDS dans la préparation d'un médicament destiné à traiter la fonction sexuelle, chez un mammifère mâle, à l'aide de très faibles doses du composé n'entraînant pratiquement pas d'augmentation des taux périphériques moyens d'estradiol au-delà des taux périphériques moyens normaux chez le mammifère mâle.
EP04780074A 2003-07-31 2004-08-02 Methodes de traitement de dysfonctionnements sexuels masculins et feminins Withdrawn EP1648471A4 (fr)

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PCT/US2004/025173 WO2005011618A2 (fr) 2003-07-31 2004-08-02 Methodes de traitement de dysfonctionnements sexuels masculins et feminins

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DE102006003512A1 (de) * 2006-01-24 2007-08-02 Bayer Schering Pharma Ag Plättchenförmige Arzneimittel zur transbukkalen Applikation von Arzneistoffen
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WO2005011618A3 (fr) 2005-12-29
JP2007512225A (ja) 2007-05-17
WO2005011617A2 (fr) 2005-02-10
US20050059615A1 (en) 2005-03-17
WO2005011618A2 (fr) 2005-02-10
EP1648471A4 (fr) 2009-05-13

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